Evidence map›Paper›PMID 37732214›Full record

ArticlebioRxiv : the preprint server for biology2023

Tauopathy severely disrupts homeostatic set-points in emergent neural dynamics but not in the activity of individual neurons.

James N McGregor, Clayton A Farris, Sahara Ensley, Aidan Schneider, Chao Wang, Yuqi Liu, Jianhong Tu, Halla Elmore, Keenan D Ronayne, Ralf Wessel and 4 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

James N McGregorDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Clayton A FarrisDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Sahara EnsleyDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Aidan SchneiderDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Chao WangDepartment of Neurology, Hope Center for Neurological Disorders, Knight Alzheimer's Disease Research Center, Washington University in Saint Louis, St. Louis, MO, USA.
Yuqi LiuDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Jianhong TuDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Halla ElmoreDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Keenan D RonayneDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Ralf WesselDepartment of Physics, Washington University in Saint Louis, St. Louis, MO, USA.
Eva L DyerCoulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
Kiran Bhaskaran-NairDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
David M HoltzmanDepartment of Neurology, Hope Center for Neurological Disorders, Knight Alzheimer's Disease Research Center, Washington University in Saint Louis, St. Louis, MO, USA.
Keith B HengenDepartment of Biology, Washington University in Saint Louis, St. Louis, MO, USA.
Washington University in St. Louis · USHope Center for Neurological Disorders · USGeorgia Institute of Technology · US

Funding

Effect of APOE on CNS Neurons: Role of LRPRF1NS090934 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2020 to 2025
$6.5M
Novel Strategies and Mechanisms to Target APOE and Alzheimer's DiseaseRF1AG047644 · NIA · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M., HYMAN, BRADLEY T. · 2019 to 2019
$3.8M
A Comparative Framework for Modeling the Low-Dimensional Geometry of Neural Population StatesR01EB029852 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI DYER, EVA · 2020 to 2020
$1.1M
Robust circuit computation in freely behaving animals.R01NS118442 · NINDS · WASHINGTON UNIVERSITY · PI HENGEN, KEITH B. · 2023 to 2024
$1.0M
NIA NIH HHS RF1 AG047644NIBIB NIH HHS R01 EB029852NINDS NIH HHS R01 NS118442NINDS NIH HHS RF1 NS090934
6 · The paper itself

Abstract

The homeostatic regulation of neuronal activity is essential for robust computation; key set-points, such as firing rate, are actively stabilized to compensate for perturbations. From this perspective, the disruption of brain function central to neurodegenerative disease should reflect impairments of computationally essential set-points. Despite connecting neurodegeneration to functional outcomes, the impact of disease on set-points in neuronal activity is unknown. Here we present a comprehensive, theory-driven investigation of the effects of tau-mediated neurodegeneration on homeostatic set-points in neuronal activity. In a mouse model of tauopathy, we examine 27,000 hours of hippocampal recordings during free behavior throughout disease progression. Contrary to our initial hypothesis that tauopathy would impact set-points in spike rate and variance, we found that cell-level set-points are resilient to even the latest stages of disease. Instead, we find that tauopathy disrupts neuronal activity at the network-level, which we quantify using both pairwise measures of neuron interactions as well as measurement of the network's nearness to

Indexed as

behaviorcriticalityhippocampushomeostasisNeurodegenerationneurophysiologysleeptau

Identifiers

PMID37732214
PMCPMC10508737
OpenAlexW4386446387

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.